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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364528Generated: October 30, 2026

p-Nitrobenzyl 7-{2-(1,2,3-thiadiazol-4-yl)-2-methoxyiminoacetamido}-3-cephem-4-carboxylate → 7-{2-(1,2,3-Thiadiazol-4-yl)-2-methoxyiminoacetamido}-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/364528

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Nitrobenzyl 7-{2-(1,2,3-thiadiazol-4-yl)-2-methoxyiminoacetamido}-3-cephem-4-carboxylateHCID 131712449—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product7-{2-(1,2,3-Thiadiazol-4-yl)-2-methoxyiminoacetamido}-3-cephem-4-carboxylic acidHCID 13171301924.8%

Reaction Steps

10% Palladium carbon (0.85 g.) was added to a solution of p-nitrobenzyl 7-{2-(1,2,3-thiadiazol-4-yl)-2-methoxyiminoacetamido}-3-cephem-4-carboxylate (syn isomer, 1.65 g.) in methanol (70 ml.) and tetrahydrofuran (90 ml.), and the mixture was subjected to catalytic reduction at room temperature under atmospheric pressure for 3.5 hours. After removing the catalyst from the reaction mixture by filtration, the filtrate was concentrated under reduced pressure. Water was added to the residue, and the mixture was adjusted to pH 7 to 8 with sodium bicarbonate, washed with ethyl acetate, adjusted to pH 1.5 with 10% hydrochloric acid, and then extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure, and the residue was pulverized with diethyl ether. The precipitates were collected by filtration and the dried to give yellow powder of 7-{2-(1,2,3-thiadiazol-4-yl)-2-methoxyiminoacetamido}-3-cephem- 4-carboxylic acid (syn isomer, 0.3 g.), m.p. 200° to 210° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04604456
Source datasetuspto-grants-1986_08
ORD IDord-c8b2846c85a5418e8550078a3e625e8c
Source noteuspto-grants-1986_08